Canonical Allele Identifier: CA1335409724

Gene: GIGYF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232747740A= , CM000664.2:g.232747740A=	GRCh38
NC_000002.11:g.233612450A= , CM000664.1:g.233612450A=	GRCh37
NC_000002.10:g.233320694A=	NCBI36
NG_011847.1:g.55436A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.167A= MANE Select	ENSP00000362664.5:p.Asn56=
ENST00000424038.2:c.167A=	ENSP00000399064.1:p.Asn56=
ENST00000373563.8:c.167A=	ENSP00000362664.4:p.Asn56=
ENST00000409196.7:c.167A=	ENSP00000387070.3:p.Asn56=
ENST00000409451.7:c.167A=	ENSP00000387170.3:p.Asn56=
ENST00000409480.5:c.167A=	ENSP00000386765.1:p.Asn56=
ENST00000409547.5:c.167A=	ENSP00000386537.1:p.Asn56=
ENST00000421433.5:c.167A=	ENSP00000402053.1:p.Asn56=
ENST00000423659.5:c.167A=	ENSP00000404195.1:p.Asn56=
ENST00000424038.1:c.167A=	ENSP00000399064.1:p.Asn56=
ENST00000425040.5:c.167A=	ENSP00000407161.1:p.Asn56=
ENST00000428883.5:c.167A=	ENSP00000402712.1:p.Asn56=
ENST00000429187.5:c.167A=	ENSP00000392991.1:p.Asn56=
ENST00000430720.5:c.167A=	ENSP00000396958.1:p.Asn56=
ENST00000440945.5:c.167A=	ENSP00000410297.1:p.Asn56=
ENST00000456491.5:c.130+37A=	ENSP00000413612.1:n.130+37A=
ENST00000463554.5:n.319A=
ENST00000629305.2:c.167A=	ENSP00000487548.1:p.Asn56=
NM_001103146.1:c.167A=	NP_001096616.1:p.Asn56=
NM_001103147.1:c.167A=	NP_001096617.1:p.Asn56=
NM_001103148.1:c.167A=	NP_001096618.1:p.Asn56=
NM_015575.3:c.167A=	NP_056390.2:p.Asn56=
NR_103492.1:n.280A=
NM_001103146.3:c.167A= MANE Select	NP_001096616.1:p.Asn56=
NM_001103147.2:c.167A=	NP_001096617.1:p.Asn56=
NM_001103148.2:c.167A=	NP_001096618.1:p.Asn56=
NM_015575.4:c.167A=	NP_056390.2:p.Asn56=